Canonical Allele Identifier: CA343553908

Gene: NPHS2

Linked Data

• gnomAD v4: 1-179575768-C-G
• MyVariant Identifiers: chr1:g.179544903C>G (hg19) ; chr1:g.179575768C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179575768C>G , CM000663.2:g.179575768C>G	GRCh38
NC_000001.10:g.179544903C>G , CM000663.1:g.179544903C>G	GRCh37
NC_000001.9:g.177811526C>G	NCBI36
NG_007535.1:g.5182G>C , LRG_887:g.5182G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367615.9:c.97G>C MANE Select	ENSP00000356587.4:p.Gly33Arg
ENST00000367615.8:c.97G>C	ENSP00000356587.4:p.Gly33Arg
ENST00000367616.4:c.97G>C	ENSP00000356588.4:p.Gly33Arg
NM_001297575.1:c.97G>C	NP_001284504.1:p.Gly33Arg
NM_014625.3:c.97G>C , LRG_887t1:c.97G>C	NP_055440.1:p.Gly33Arg
XM_005245483.2:c.97G>C	XP_005245540.1:p.Gly33Arg
XM_006711529.2:c.97G>C	XP_006711592.1:p.Gly33Arg
XM_005245483.3:c.97G>C	XP_005245540.1:p.Gly33Arg
XM_017002298.1:c.97G>C	XP_016857787.1:p.Gly33Arg
XM_017002299.1:c.97G>C	XP_016857788.1:p.Gly33Arg
NM_001297575.2:c.97G>C	NP_001284504.1:p.Gly33Arg
NM_014625.4:c.97G>C MANE Select	NP_055440.1:p.Gly33Arg